The Food and Drug Administration (FDA) and the Department of Science and Technology (DOST) have joined forces to simplify regulatory processes for health technologies, aiming to accelerate market entry while maintaining public health safety. The collaboration includes establishing a green lane for expedited registration of locally developed products, streamlining clinical trial approvals, and enhancing capacity building through initiatives like the Balik Scientist Program.
To support the growth of local health innovations, the Food and Drug Administration and the Department of Science and Technology have come together to simplify regulatory processes, paving the way for quicker market entry of health technologies while safeguarding public health.The two agencies convened on Jan.
FDA Director General Samuel Zacate reaffirmed the agency’s commitment to regulatory streamlining, emphasizing the need to strike a balance between efficiency and public health protection.“The FDA is dedicated to streamlining regulatory processes to help local technologies reach the market faster without compromising the safety, efficacy, and quality of health products,” Zacate said.Meanwhile, DOST Secretary Dr. Renato U. Solidum Jr.
HEALTHTECHNOLOGY REGULATION INNOVATION CAPACITYBUILDING PHILIPPINE
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